Nouman Rafiq, Waqar A.A. Syed, Aulia Rifada, M. Asad Ghufran, Ijaz-Ur-Rehman Shah, Ahsan Ali and Wiqar Hussain Shah
We report a simple approach for synthesizing monodispersed, crystalline and size-tunable tin sulfide nanoparticles for environment friendly next generation solar cell applications. Both SnS and SnS2 nanoparticles could be a potential nanomaterial for solar cells. The structural, morphological, thermal and optical properties were investigated using X-ray diffraction (XRD), scanning electron microscopy (SEM), thermal gravimetric analysis (TGA), diffuse reflectance spectroscopy (DRS) and Fourier transform infrared spectroscopy (FT-IR). The XRD spectra revealed hexagonal and orthorhombic phases of SnS and SnS2 nanoparticles, respectively, where the grains size ranged from 11 nm to 30 nm. The weight percentage as a function of temperature was determined using TGA analysis. Functional groups were observed by FT-IR. The energy bandgap was determined as 1.41 eV showing usefulness of the nanoparticles in next generation environmental friendly solar energy applications.
Pure CdO nanopowder and CdO-Fe3O4 nanocomposite were synthesized by a cost effective chemical method, and the samples were characterized by XRD, SEM, TEM, FT-IR, UV-Vis-NIR and PL. Also, magnetic and photocatalytic properties of the synthesized samples were studied. XRD patterns of the composite confirm the presence of diffraction peaks related to both CdO and Fe3O4. EDX spectrum confirms the presence of the elements Cd, O and Fe in the composite. Peaks related to Cd–O and Fe–O bonds were observed respectively at 688 cm−1 and 592 cm−1 in the FT-IR spectrum. The paramagnetic behavior of pure CdO becomes ferromagnetic when coupled with Fe3O4. The composite exhibited a high photodegradation efficiency of 92.85 % against the degradation of methylene blue dye under visible light radiation.
In this research work, we prepared γ-Fe2O3 nanoparticles by thermal-decomposition of Fe3O4. The Fe3O4 nanoparticles were synthesized via co-precipitation method at room temperature. This simple, soft and cheap method is suitable for preparation of iron oxide nanoparticles (γ-Fe2O3; Fe3O4). The samples were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), transmission electron microscopy (TEM), vibrating sample magnetometer and differential scanning calorimeter (DSC). The XRD and FT-IR results indicated the formation of γ-Fe2O3 and Fe3O4 nanoparticles. The TEM images showed that the γ-Fe2O3 and Fe3O4 were spherical, and their size was 18 and 22 nm respectively. Magnetic properties have been measured by VSM at room temperature. Hysteresis loops showed that the γ-Fe2O3 and Fe3O4 nanoparticles were super-paramagnetic.
Meiry G. F. Rodrigues, Antonielly S. Barbosa, Ana C. F. Coriolano, Edjane F. B. Silva and Antonio S. Araujo
The hydrothermal synthesis of MCM-22 zeolite was carried out using silica, sodium aluminate and hexamethyleneimine, under static conditions at 150 °C for a period of 10 days, followed by washing with deionized water, drying overnight and calcination at 650 °C. The obtained material was characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR) and scanning electron microscopy (SEM). The XRD analysis evidenced that MCM-22 presented a well defined MWW structure. The FT-IR spectrum confirmed the efficiency of the hexamethyleneimine as an organic template used to direct the structure of the MCM-22 zeolite under static conditions. The SEM image indicated that the particles are spherical in shape, with a diameter of ca. 10 μm. The acid properties of the MCM-22 zeolite, as determined by n-buthylamine adsorption, were investigated in the temperature ranges of 105 to 300 °C and 300 to 525 °C, relative to medium and strong acid sites, respectively.
The effect of different fabrication techniques on the formation of electroactive β-phase polyvinylidene fluoride (PVDF) has been investigated. Films with varying concentration of PVDF and solvent - dimethyl formamide (DMF) were synthesized by tape casting and solvent casting techniques. The piezoelectric β-phase as well as non polar β-phase were observed for both the tape cast and solvent cast films from X-ray diffraction (XRD) micrographs and Fourier transform infra-red spectroscopy (FT-IR) spectra. A maximum percentage (80 %) of β-phase was obtained from FT-IR analysis for a solvent cast PVDF film. The surface morphology of the PVDF films was analyzed by FESEM imaging. The dielectric properties as a function of temperature and frequency and the ferroelectric hysteresis loop as a function of voltage were measured. An enhancement in the value of the dielectric constant and polarization was obtained in solvent cast films.
Sahebali Manafi, Simin Tazikeh and Sedigheh Joughehdoust
Synthesis of indium tin oxide (ITO) nanoparticles by reflux method without chlorine contamination at different pHs, temperatures, solvents and concentrations has been studied. Indium chloride, tin chloride, water, ethanol and Triton X-100 were used as starting materials. Structure, size, surface morphology and transparency of indium tin oxide nanoparticles were studied by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM) and UV-Vis spectrophotometry. XRD patterns showed that 400 °C is the lowest temperature for synthesis of ITO nanoparticles because metal hydroxide does not transform to metal oxide in lower temperature. FT-IR results showed the transformation of hydroxyl groups to oxide. SEM images showed that pH is the most important factor affecting the nanoparticles size. The smallest nanoparticles (40 nm) were obtained at pH = 8.8. The size of crystallites was decreased by lowering of concentration (0.025 M).
The solid acidic nanocatalyst fly-ash:H3PO4 was prepared and characterized by FT-IR, SEM, EDS and TEM analysis. This catalyst was utilized for aldol condensation, coupling and cyclization reaction. The effect of catalytic activity of this fly-ash:H3PO4 nanocatalyst was studied with the obtained yield of products under solvent-free conditions. In this synthetic reaction the obtained yields were more than 95 %.
Factors influencing the reaction of chemical polymerization during aniline doping with hydrochloric acid (HCl) have been studied in this work. The optimal parameters for the preparation of polyaniline were determined as follows: aniline concentration - 4 mass %, molar ratios of oxidant (NH4)2S2O8:aniline - 1.2:1 and 1.3:1, the concentration of dopant - 1 mol/L. Fourier transform infrared spectroscopy (FT-IR) was applied to characterize the structure of polyaniline.
Božana Čolović, Danilo Kisić, Bojan Jokanović, Zlatko Rakočević, Ilija Nasov, Anka Trajkovska Petkoska and Vukoman Jokanović
Thin films of titanium oxides, titanium oxynitrides and titanium nitrides were deposited on glass substrates by the methods of direct current (DC) and pulsed magnetron sputtering and cathodic arc evaporation. Phase analysis of the deposited films by X-ray diffraction (XRD) and Fourier-transform infrared spectroscopy (FT-IR) showed the presence of phases with various Ti oxidative states, which indicated a high concentration of oxygen vacancies. The films morphology was investigated by scanning electron microscopy (SEM). Investigations of the films wettability, either with water or ethylene glycol, showed that it depends directly on the concentration of oxygen vacancies. The wettability mechanism was particularly discussed.